Sr. Research Program Coordinator HPRC
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Job Location:
Oklahoma City, OK - USA
Monthly Salary:
Not Disclosed
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Required Education: Bachelors Degree in a Health Profession Physical Science Biological Science Nursing or related discipline AND:
- 5 years experience in clinical practice nursing clinical research coordination or related field.
Certifications or Licenses: Active state licensure required for Registered Nurses and Physician Assistants (may be required based on research area)
Skills:
- Strong knowledge of clinical research practices and regulatory requirements
- Excellent patient care and assessment skills.
- Proficient in data management and use of electronic medical/research records.
- Effective communication and interpersonal skills.
- Demonstrated leadership and staff supervision abilities.
- Ability to multitask and work independently in a fast-paced research environment
Working Conditions:
- Environmental: Standard Office Environment
- Physical: Sit for prolonged periods. Communicate effectively and listen. Use of computer.
Why You Belong at the University of Oklahoma:The University of Oklahoma values our communitys unique talents perspectives and experiences. At OU we aspire to harness our innovation creativity and collaboration for the advancement of people everywhere. You Belong Here!
Equal Employment Opportunity Statement:The University in compliance with all applicable federal and state laws and regulations does not discriminate on the basis of race color national origin sex sexual orientation marital status genetic information gender identity/expression (consistent with applicable law) age (40 or older) religion disability political beliefs or status as a veteran in any of its policies practices or procedures. This includes but is not limited to admissions employment housing financial aid and educational services.
Required Attachments
Documents required for this position are listed under the Required Attachments section of this job listing. You will be required to upload and attach these documents in the application process.
OU Health Stephenson Cancer Center is Oklahomas only National Cancer Institute (NCI)-Designated Cancer Center and one of only 73 NCI-Designated Cancer Centers in the United States. This highly competitive accreditation ensures that our patients receive the highest standard of care and have access to the most advanced cancer treatment options.
At the Stephenson Cancer Center we have an exciting new job opportunity that could be right for you! The Sr. Research Program Coordinator at the Health Promotion Research Center involves identifying and recruiting eligible participants conducting clinical assessments and research testing managing data ensuring regulatory compliance and serving as a key liaison between clinical research and administrative teams.
Learn more about the Health Promotion Research Center here.
Duties:
- Identifies recruits and schedules patients who may be eligible for the research study based on inclusion/exclusion criteria.
- Performs initial clinical assessments including medical history.
- Completes necessary patient documentation and data collection forms.
- Conducts research-related tests and supervises participant exercise training sessions as applicable.
- Provides potential participants with detailed study information.
- Obtains and documents informed consent in accordance with IRB and regulatory guidelines.
- Serves as a point of contact and clinical resource for the research team.
- Coordinates communication among laboratory staff and other collaborators.
- Assists with accurate data entry data management and preliminary data analysis in support of study goals.
- Coordinates and executes follow-up visits including assessments and monitor data review.
- Manages and oversees home-based training programs through scheduled phone calls and remote monitoring.
- Attends research team and department meetings.
- May present study updates data findings or operational needs as required.
- Provides leadership in ensuring protocol adherence.
- Trains supervises and evaluates research personnel.
- Assigns and monitors workloads and schedules.
- Performs related duties as assigned to successfully fulfill the function of the position.
Required Experience:
Senior IC
Key Skills
- Project / Program Management
- Program Management
- Developmental Disabilities Experience
- Organizational skills
- Data Collection
- Meeting Facilitation
- Utilization Review
- Administrative Experience
- Program Development
- Public Speaking
- Supervising Experience
- Social Work
